3 Ways Medical Device Companies Working Remote are Leveraging QMS Software to Foster Innovation and Collaboration

As events surrounding the coronavirus (COVID-19) continue to unfold, medical device companies are finding themselves facing unforeseen challenges, whether that be centralized teams now being forced to collaborate and access information remotely, clinical trials being delayed, or a myriad of other issues caused by the "new normal".  

Based on data-driven insights from medical device industry professionals in the 2020 State of Medical Device Product Development & Quality Management Report, we know medical device companies’ ability to collaborate will be disrupted based on the fact that:

  • 71% of respondents already reported the company's quality system data was not easily accessible in real-time
  • Only 7% of companies find themselves to be highly efficient during the design and development process of bringing a device to market, and this inefficiency will be further compounded for remote teams
  • 55% of respondents indicates that managing a pile of documents was one of the biggest challenges in managing design controls, and that pile of documents now becomes even less accessible and "connected" in this new world
  • On average, respondents said it takes 212 hours (5 weeks) to compile a DHF, and that's when all the information and people were in one location

And yet companies that indicated that they were using best-in-class software for managing product development and quality activities are:

  • 3x more likely to call themselves “highly efficient” when bringing a device to market
  • 2x as likely to feel “very confident” about demonstrating total lifecycle traceability in the event of an unannounced audit
  • 2x as likely to need less than one day to prepare for an audit

This in-depth webinar will cover how companies using turn-key, best-in-class QMS software are able to remain agile in order to innovate and outperform the competition.

Watch the webinar

4-23-20 webinar
Specifically, this webinar will cover:
  • Leveraging a single source of truth for design control and risk management activities to drive collaboration and accelerate device clearance timelines
  • How a connected quality system enables demonstrating closed-loop traceability in order to assure near real-time audit readiness
  • How to streamline quality processes and document control activities across internal team and external stakeholders
  • Front-line customer stories regarding paperless ISO and MDSAP audit experiences that wowed auditors
  • How to easily get started in taking a digital-first approach to quality, without a significant internal resource commitment or about worrying burdensome system validation
  • Q&A session
Who Should Attend?
  • Product Development and R&D Professionals
  • Quality Assurance & Regulatory Affairs Professionals
  • Medical Device Executives & Leadership Teams
Register Now  

Hosted by

Moderator/Presenter: Jon Speer

Founder, Greenlight Guru


About Greenlight Guru

Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.

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